电化学
再生(生物学)
阴极
电池(电)
相(物质)
化学
化学工程
电极
金属
纳米技术
材料科学
熔盐
资源回收
化学物理
阳极
氧气
动能
环境污染
析氧
气相
兴奋剂
盐(化学)
四面体
电子结构
作者
Yuan‐Meng Li,Yujia He,Kai Jia,Haojie Dong,Xinyu Zhang,Hao Qin,Lingling Hu,Hao Zhang,Zhao‐Kun Guan,Si‐Fan Chen,Mengting Liu,Bing Xiao,Shujiang Ding,Kai Xi,Pengfei Wang
标识
DOI:10.1002/ange.202520448
摘要
Abstract The direct regeneration of cathodes is an effective technique to address resource waste and environmental pollution caused by spent lithium‐ion batteries (LIBs). However, Li + migration within the rock‐salt phase of degraded LiNi 0.5 Co 0.2 Mn 0.3 O 2 cathodes follows an energetically unfavorable 2‐transition metal (2‐TM) transport pathway (tetrahedral sites between face‐sharing octahedra), creating a kinetic barrier that fundamentally limits direct regeneration. A Na‐based molten salt pretreatment is applied to introduce Na atoms into the unoccupied tetrahedral sites of the rock‐salt phase, which alters the electronic state distribution of bridged oxygen anions and reduces super‐exchange interactions between TM atoms in adjacent layers, thereby triggering a phase transformation from rock‐salt to targeted layered structure. Consequently, the Li + migration pathway shifts from a high‐energy 2‐TM route to a more favorable low‐barrier 1‐TM route, enabling efficient lithiation and complete restoration of the cathode. The regenerated materials exhibit high structural uniformity and excellent electrochemical performance, achieving 78% capacity retention after 500 cycles. This study provides an insightful perspective on direct LIB recycling by regulating super‐exchange interactions within the degraded cathode structures.
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